Table 1 Detailed information of RNA-seq data

Sequencing data statistics

Clean reads

20,112,132

27,809,393

25,022,722

25,669,474

25,182,500

23,361,247

Clean bases

6,011,496,948

8,314,175,984

7,490,345,612

7,672,294,656

7,525,008,224

6,982,459,062

GC Content

42.66%

42.07%

42.46%

41.79%

41.77%

41.75%

% ≥ Q30

94.52%

94.46%

94.43%

94.94%

95.01%

94.92%

Based on selected reference genome, statististic of sequence alignment results between sample sequencing data

Total Reads

40,224,264

55,618,786

50,045,444

51,338,948

50,365,000

46,722,494

Mapped Reads

38,466,134(95.63%)

53,225,213(95.70%)

48,026,349(95.97%)

48,812,363(95.8%)

47,848,224(95.00%)

44,748,280(95.77%)

Uniq Mapped Reads

35,062,965(87.17%)

50,662,268(91.09%)

46,241,168(92.40%)

47,515,584(92.55%)

46,601,110(92.53%)

43,612,976(93.34%)

Multiple Map Reads

3,403,169(8.46%)

2,562,945(4.61%)

1,785,181(3.57%)

1,296,779(2.53%)

1,247,114(2.48%)

1,135,304(2.43%)

Reads Map to ‘ + ’

18,558,770(46.14%)

26,181,517(47.07%)

23,744,948(47.45%)

24,259,222(47.25%)

23,771,258(47.20%)

22,257,873(47.64%)

ReadsMap to ‘-’

19,022,283(47.29%)

26,451,663(47.56%)

23,917,058(47.79%)

24,327,689(47.39%)

23,850,045(47.35%)

22,312,867(47.76%)